SCHEMBL1347723

SCHEMBL1347723

O=C(Cl)Oc1ccc(-c2ccccc2)cc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 4/20 0.53
MEN1 O00255 3/20 0.53
SMN1; SMN2 Q16637 3/20 0.51
LMNA P02545 2/20 0.51
NPSR1 Q6W5P4 1/20 0.51
FABP7 O15540 1/20 0.49
FABP3 P05413 1/20 0.49
FABP5 Q01469 1/20 0.49
KDM4E B2RXH2 1/20 0.49
NPC1 O15118 1/20 0.49
RAB9A P51151 1/20 0.49
GAA P10253 2/20 0.48
CYP1A2 P05177 1/20 0.48
CYP2C9 P11712 1/20 0.48
PKM P14618 1/20 0.48
CYP2C19 P33261 1/20 0.48
TDP1 Q9NUW8 2/20 0.46
MAPT P10636 2/20 0.46
HSD17B10 Q99714 1/20 0.46
CA1 P00915 1/20 0.44

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL6565732 0.91 HSD17B10 (0.47) KMT2AMEN1SMN1; SMN2LMNANPSR1
Benzene SCHEMBL7925278 0.86 TDP1 (0.50) KDM4ERAB9ATDP1MAPTHSD17B10
SCHEMBL3302 0.86 TDP1 (0.50) KDM4ERAB9ATDP1MAPTHSD17B10
SCHEMBL370622 0.86 TDP1 (0.50) KDM4ERAB9ATDP1MAPTHSD17B10
SCHEMBL27902340 0.84 TDP1 (0.48) KDM4ERAB9ATDP1MAPTHSD17B10
SCHEMBL27326182 0.84 TDP1 (0.48) KDM4ERAB9ATDP1MAPTHSD17B10
Ammonia Solution, Strong SCHEMBL28185209 0.84 TDP1 (0.48) KDM4ERAB9ATDP1MAPTHSD17B10
SCHEMBL10975650 0.84 TDP1 (0.48) KDM4ERAB9ATDP1MAPTHSD17B10
Hydrochloric Acid SCHEMBL3896561 0.84 TDP1 (0.48) KDM4ERAB9ATDP1MAPTHSD17B10
SCHEMBL11224568 0.84 TDP1 (0.48) KDM4ERAB9ATDP1MAPTHSD17B10

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 36 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2766450-A1 SUBSTITUTED AMINO ALCOHOLS AS CHIRAL DOPANTS FRAUNHOFER-GESELLSCHAFT zur Förderung der angewandten Forschung e.V. (DE) 2014-08-20 EP disclosed
WO-2013053752-A1 SUBSTITUTED AMINO ALCOHOLS AS CHIRAL DOPANTS Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. (DE) 2013-04-18 WO disclosed
US-8173700-B2 Salts of substituted allophanates and their use in drugs GRUENENTHAL GMBH (DE) 2012-05-08 US disclosed
US-8173700-B2 Salts of substituted allophanates and their use in drugs GRUENENTHAL GMBH (DE) 2012-05-08 US disclosed
US-8173700-B2 Salts of substituted allophanates and their use in drugs GRUENENTHAL GMBH (DE) 2012-05-08 US disclosed
US-8063021-B2 Ketolide anti-infective compounds KOSAN BIOSCIENCES INCORPORATED (US) 2011-11-22 US disclosed
EP-2242747-A1 SUBSTITUTED IMIDAZOLIDINE-2,4-DIONES, METHOD FOR THE PRODUCTION THEREOF, MEDICAMENTS CONTAINING SAID COMPOUNDS AND USE THEREOF Sanofi-Aventis (FR) 2010-10-27 EP disclosed
EP-2111236-A2 NOVEL CASCADE POLYMER COMPLEXES, METHOD FOR THEIR PRODUCTION AND PHARMACEUTICAL AGENTS CONTAINING THE SAME Bayer Schering Pharma Aktiengesellschaft (DE) 2009-10-28 EP disclosed
WO-2009097997-A1 SUBSTITUTED IMIDAZOLIDINE-2,4-DIONES, METHOD FOR THE PRODUCTION THEREOF, MEDICAMENTS CONTAINING SAID COMPOUNDS AND USE THEREOF SANOFI-AVENTIS (FR) 2009-08-13 WO disclosed
EP-1888514-B1 SALTS OF SUBSTITUTED ALLOPHANATES AND THEIR USE IN DRUGS GRUENENTHAL GMBH (DE) 2009-03-18 EP disclosed
EP-0466183-A1 Cyclosiloxanes with mesogenic side groups Consortium für elektrochemische Industrie GmbH (DE) 1992-01-15 EP disclosed
EP-0368176-A1 Esters of carboximidic acid, their preparation, and their use as pesticides CIBA-GEIGY AG (CH) 1990-05-16 EP disclosed
EP-0219756-A1 Acrylic amides SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1987-04-29 EP disclosed
EP-0061013-B1 PROCESS FOR THE PREPARATION OF POLYISOCYANATES BAYER AG (DE) 1984-06-27 EP disclosed
EP-0041043-B1 PROCESS FOR THE PREPARATION OF DERIVATIVES OF ALKENYL BENZENE OR ALKENYL NAPHTHALENE CIBA-GEIGY AG (CH) 1983-11-09 EP disclosed
EP-0040177-B1 PROCESS FOR THE PREPARATION OF BENZENE OR NAPHTHALENE ALKENYL CARBOXYLIC ACID DERIVATIVES CIBA-GEIGY AG (CH) 1983-07-20 EP disclosed
US-4376731-A 2-NITRILES THEREOF BOEHRINGER MANNHEIM GMBH (DE) 1983-03-15 US disclosed
EP-0061013-A1 Process for the preparation of polyisocyanates BAYER AG (DE) 1982-09-29 EP disclosed
EP-0041043-A1 Process for the preparation of derivatives of alkenyl benzene or alkenyl naphthalene CIBA-GEIGY AG (CH) 1981-12-02 EP disclosed
EP-0040177-A1 Process for the preparation of benzene or naphthalene alkenyl carboxylic acid derivatives CIBA-GEIGY AG (CH) 1981-11-18 EP disclosed